Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene

American Journal of Ophthalmology

Volumn 121, Issue 6, 1996, Pages 623-629

  Hoyng, C B ^a   Heutink, P ^a   Testers, L ^a   Pinckers, A ^a   Deutman, A F ^a   Oostra, B A ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; DNA; PERIPHERIN; TRYPTOPHAN;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; GENE MUTATION; HUMAN; MALE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RETINA MACULA AGE RELATED DEGENERATION;

EID: 0029942002     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(14)70627-0     Document Type: Article

References (18)

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